Tag | Content |
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EnhancerAtlas ID | HS161-04491 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr13:110669300-110670730 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr13:110669503-110669523 | CCCCAACCCAACTCCACAGG | + | 6.23 | STAT3 | MA0144.2 | chr13:110669416-110669427 | CTTCCCAGAAA | - | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_36176 | chr13:110662641-110671312 | HMEC | SE_52128 | chr13:110668422-110671379 | Skeletal_Muscle_Myoblast | SE_63892 | chr13:110666468-110671520 | HSMM |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I110010 | chr13 | 110662562 | 110671114 |
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Enhancer Sequence | CTAGCTACAA CATAATACTA TCTAACAGAG TTACCTCAGT ATAAGATCTT AGAAATGAAA 60 GTGTGGGTCT CAGGGTATAC ATATTTTAAA GACTTTATAT TGTGATTATT AATTTGCTTC 120 CCAGAAAGTT TGTATAAATA TTAGCTCTGA CCGGCTGTGT GCAAGAGTAC CAGTTAGCCA 180 CAACCACTGT TGAGTATTAC CCACCCCAAC CCAACTCCAC AGGGACGAAT ACACTGCATT 240 GCTGTTTTCA TTCCCCTTTC TTTGCTTACT GATAATTTCA AGGAGGGTTT GGTTTCAAGT 300 GTTTTGTTGG CTTATATTTT CCTTCTGTGA ATTTGTCATT TATATATTCT ATTTGCTGCT 360 TCTTTTAAGT TGAAGAATTG TTAGAAGAAA TCATGAAGAC AATTGCTGGG TTTGAATTGA 420 TGCTTGCAGC TTCTGGAGAC ATTTGTCTTG AGTGAAAGCA TCAGGTGAGA GCTCTGAGAG 480 CAGGTGAGCC AAGGCTGGGG AAGCGTCCTA AGCCAGGGGA GCTCTCCCAG CTGGTGCTGC 540 ACGTGCGCTC CAGAGGGAAG GCTCTTGATG CCTCCCGTGC TGCTTGGGGC CCTTCTTCAG 600 GGAAGTGAGG ATGTTTCTCC CAGGATTCAG ATACCAGAAG CAGGATGACC ACACCTCTTT 660 CCTCTCATTC CTGAGGTTCC CAGTGCGTCC GCCTCCTCAC ATTCCTATGT GTTTGCCTCA 720 TCTAGTCCAT GACTGGTACC TTTTTTCCTA CAGAAAAACT GAAACAACTA TGCAGTTTTC 780 CCCATTCCCA TCTCAGGTTC GGGGCAGCTT AATTAGAAAG TGTCAGTAAA TGTGCTTTGA 840 GATCCTTAGA AGATGAGTTG AGTGGTCATT CCCCAAGACC TCGGCATCGG TATCGCCAAG 900 GCGGCTTTGC AGTAAATGTT AGGGGAAGAA TGGAGGGCCA TTTGTGTTGT GCAGAGGAAG 960 ACAAAATGTC CATCACATAA CTGAACACGA CTGAGATGGT CCAATTACTT TGTCTCTCTG 1020 GCTTTTTTCA ATAGTGCAAA GGAATGGTGA TTAGGCAAGA ATCCTAAACA GGAGAAACCC 1080 AAGTCCGTTC TGAGGTGCGT TGTGCATGGA GGCTGCTGGG CAGCACCAGT CATGCGGTAG 1140 TGTACAACAG ACCTTCAACA CCATCAGCAT AATGATCACC CACCCGCTCT GTGCCCAGCA 1200 TGGAACCACG GCCGGAGCAA GCCCGGCTGT GAGCATTCAG TGTCTTACCC AGATGCCAGG 1260 AGCCTGTGTG TCTTGGGTCG GTGTCTCTCT CCCCCACTTC CTGGCCAGGC TCTTGCCCTC 1320 TCATGTACGA ATCACTAAGC ACGCTCCATC CTCAGCCTCA GCAGCAGCCT CTGCCCCACT 1380 GTCCAGTTCT ATTTCTGCAG TACCTCACCA TCCTTATTGG AGACAGCCCT 1430
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